dc.contributor.author | Keskin, S. | |
dc.contributor.author | Yildiz, I. | |
dc.contributor.author | Sen, F. | |
dc.contributor.author | Aydogan, F. | |
dc.contributor.author | Kilic, L. | |
dc.contributor.author | Ekenel, M. | |
dc.contributor.author | Aykan, F. | |
dc.date.accessioned | 2019-08-13T12:10:23Z | |
dc.date.accessioned | 2019-08-13T16:03:10Z | |
dc.date.available | 2019-08-13T12:10:23Z | |
dc.date.available | 2019-08-13T16:03:10Z | |
dc.date.issued | 2013 | |
dc.identifier.issn | 1699-048X | |
dc.identifier.uri | https://dx.doi.org/10.1007/s12094-012-0942-8 | |
dc.identifier.uri | http://hdl.handle.net/11446/3016 | |
dc.description | WOS: 000318290100010 | en_US |
dc.description | PubMed ID: 23054756 | en_US |
dc.description.abstract | The aim of this retrospective study (from January 2007 to December 2011) was to investigate the efficacy and tolerability of mDCF schedule for chemotherapy-na < ve AGC patients. Patients (n = 54) with locally inoperable or distant metastasis and performance status of 0-2 were eligible. The triplet combination chemotherapy consisting of docetaxel 60 mg/m(2) on day 1, cisplatin 60 mg/m(2) on day 1, and 5-fluorouracil 600 mg/m(2) for 5 days of continuous infusion were administered every 21 days, up to nine cycles. Prophylactic G-CSF was not allowed. In all, 36 (67 %) patients were male and 18 (33 %) were female; median age was 59 years. The majority of patients (n = 46, 85 %) had metastatic disease and 8 (15 %) of them had locally advanced disease. Liver metastasis and peritonitis carcinomatosa were found in 20 (43 %) and 18 (39 %) of the 46 cases, respectively. The median cycle of chemotherapy was 6. In assessing 50 patients for response evaluation, one had complete response. Partial response was achieved in 27 (54 %) patients. Seventeen patients (34 %) had stable disease and 5 (10 %) had progressive disease, while 4 % (n = 2) and 11 % (n = 6) of the patients developed severe (grade 3-4) neutropenia and anemia, respectively. During the median follow-up time (6.9 months, range 0.4-24), 28 (52 %) patients died. The overall and progression-free survival were 10.7 [95 % CI 8.9-12.4] and 6.8 [95 % CI 5.8-7.8] months, respectively. Although this was not a prospective comparative study, the mDCF regimen seems to be as effective as the original DCF in AGC with acceptable and manageable side effects. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | SPRINGER | en_US |
dc.identifier.doi | 10.1007/s12094-012-0942-8 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Modified DCF | en_US |
dc.subject | Advanced gastric cancer | en_US |
dc.subject | Efficacy | en_US |
dc.subject | Adverse effect | en_US |
dc.subject | Survival | en_US |
dc.title | Modified DCF (mDCF) regimen seems to be as effective as original DCF in advanced gastric cancer (AGC) | en_US |
dc.type | article | en_US |
dc.relation.journal | CLINICAL & TRANSLATIONAL ONCOLOGY | en_US |
dc.department | DBÜ | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.volume | 15 | en_US |
dc.identifier.startpage | 403 | en_US |
dc.identifier.endpage | 408 | en_US |
dc.contributor.authorID | 0000-0002-5569-0913 | en_US |
dc.contributor.authorID | 0000-0002-5472-3218 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.department-temp | [Keskin, S. -- Yildiz, I. -- Sen, F. -- Aydogan, F. -- Kilic, L. -- Ekenel, M. -- Sakar, B. -- Aykan, F.] Istanbul Univ, Inst Oncol, Dept Med Oncol, TR-34093 Istanbul, Turkey -- [Saglam, S.] Istanbul Bilim Univ, Dept Med Oncol, Istanbul, Turkey -- [Disci, R.] Istanbul Univ, Fac Med, Dept Publ Hlth, TR-34093 Istanbul, Turkey | en_US |